期刊文献+

增龄条件下Wnt/β-catenin信号通路在骨髓间充质干细胞中的变化

The changes of Wnt/β-catenin signaling pathway in bone marrow mesenchymal stem cells under aging condition
下载PDF
导出
摘要 目的:研究增龄条件下骨髓间充质干细胞(bone marrow mesenchymal stem cells,BMSCs)的增龄性改变及Wnt/β-catenin信号通路在增龄过程中的变化。方法:选用3月龄及18月龄的SD大鼠,双能X线检测股骨密度;分离培养BMSCs,SA-β-Gal染色分析3月龄组及18月龄组细胞衰老情况;实时定量PCR技术检测端粒酶(telomerase reverse transcriptase,TERT)mRNA表达;采用免疫酶联吸附试验检测肿瘤坏死因子(TNF-α)及白介素6(IL-6)的分泌情况;Western Blot法检测Wnt信号通路核心蛋白β-catenin在细胞浆及细胞核中的表达;实时定量PCR检测Wnt通路关键基因LEF-1、TCF-4的表达。结果:18月龄组大鼠股骨密度显著低于3月龄组;SA-β-Gal阳性表达细胞随年龄增加而增加,TERT表达水平随年龄增加而显著降低;18月龄组BMSCs TNF-α及IL-6的分泌量显著高于3月龄BMSCs;18月龄组BMSCs细胞核及细胞浆中β-catenin表达量较3月龄BMSCs均呈增高趋势;18月龄组BMSCs LEF-1的基因表达水平较3月龄BMSCs上升1.6倍,TCF-4的基因表达水平也上升3.12倍。结论:随着年龄的增加BMSCs分泌的炎症因子含量增加,导致Wnt/β-catenin信号通路活化进而影响干细胞的生物学功能。 Objective: To investigate the changes of bone marrow mesenchymal stem cells(BMSCs) and the changes of Wnt/β-catenin signaling pathway under aging condtion. Methods: 3-month-old and 18-month-old were used in our study,the femur density were detect by dual energy X-ray. We isolated BMSCs from bone marrow and then the SA-β-Gal expression was analyzed to assess the cell senescence. The expression of telomerase reverse transcriptase(TERT) mRNA was detected by real-time quantitative PCR. The secretion of tumor necrosis factor-α(TNF-α) and interleukin-6(IL-6) was detected by immuno-enzyme-linked immunosorbent assay. Western blot was used to detect the expression of β-catenin in the cytoplasm and nucleus. Real-time quantitative PCR was used to detect the expression of LEF-1 and TCF-4. Results: The femur density in the 18-month-old group was significantly lower than that in the 3-month-old group. The expression of SA-β-Gal positive cells increased in BMSCs(18-month-old group) compared with 3-month-old group, however, the expression of TERT was significantly decreased in BMSCs(18-month-old group). The secretion of TNF-α and IL-6 in BMSCs was significantly increased in 18-month-old group than in 3-month-old group. The expression of β-catenin in the nucleus and cytoplasm of BMSCs in 18-month-old group was higher than that in 3-month-old BMSCs group. The expression level of group LEF-1 in the 18-month-old group was 1.6 times higher than that of the 3-month-old group, and the gene expression level of TCF-4 also increased 3.12 times than that of the 3-month-old group. Conclusion: With the increase of age, the content of inflammatory cytokines secreted by BMSCs were increased, which led to the activation of Wnt/β-catenin signaling pathway and then affect the biological function of BMSCs.
出处 《中华老年口腔医学杂志》 2018年第1期6-11,共6页 Chinese Journal of Geriatric Dentistry
基金 国家自然科学基金(项目编号:31670998 51473175) 北京市科技新星计划(项目编号:Z141107001814101)
关键词 增龄 WNT通路 骨髓间充质干细胞 Aging bone marrow mesenchymal stem cells Wnt signaling pathway
  • 相关文献

参考文献1

二级参考文献12

  • 1Seo BM, Miura M, Gronthos S, et al. Investigation of multipotent postnatal stem cells from human periodontal ligament[J]. Lancet, 2004, 364:149-155.
  • 2Yang N, Wang G, Hu C, et al.Tumor necrosis factor a suppresses the mesenchymal stem cell osteogenesis promoter miR-21 in estrogen deficiency-induced osteoporosis [J].J BoneMiner Res, 2013, 28(3):559-573.
  • 3Liu Y, Liu W, Hu C, et al.MiR-17 modulates osteogenic differentiation through a coherent feed-forward loop in mesenchymal stem cells isolated from periodontal ligaments of patients with periodontitis[J]. Stem Cells, 2011, 29(11): 1804-1816.
  • 4Ishitani T, Kishida S, Hyodo-Miura J, et al. The TAK1- NLK mitogen-activated protein kinase cascade functions in the Wnt-5a/Ca (2+) pathway to antagonize Wnt/be- ta-catenin signaling[J]. Mol Cell Biol, 2003, 23 : 131-139.
  • 5Liu G, Vijayakumar S, Grumolato L, et al. Canonical Wnts function as potent regulators of osteogenesis by human mes- enchymal stem cells[J]. J Cell Biol, 2009, 185 : 67-75.
  • 6Chang J, Sonoyama W, Wang Z, et al. Noncanonical Wnt-4 signaling enhances bone regeneration of mesenchymal stem cells in craniofacial defects through activation of p38 MAPK[J]. J Biol Chem, 2007, 282:30938-30948.
  • 7Liu W, Konermann A, Guo T, et al. Canonical Wnt signaling differently modulates osteogenic differentiation of mesenchymal stem cells derived from bone marrow and from periodontal ligament under inflammatory conditions [J]. Bioctfim Biophys Acta, 2014, 1840(3): 1125-1134.
  • 8Slusarski DC, Pelegri F. Calcium signaling in vertebrate embryonic patterning and morphogenesis [J]. Dev Biol, 2007, 307(1):1-13.
  • 9Suzawa M, Takada I, Yanagisawa J, et al. Cytokines suppress adipogenesis and PPAR-gamma function through the TAK1/TAB1/NIK cascade[J]. Nat Cell Biol, 2003, 5 (3): 224-230.
  • 10Katoh M. STAT3-induced WNT5A signaling loop in embryonic stem cells, adult normal tissues, chronic persistent inflammation, rheumatoid arthritis and cancer [J]. Int J Mol Med, 2007, 19:273-378.

共引文献10

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部